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Aromatic L-Amino acid decarboxylase deficiency: A new case from Turkey with a novel mutation
Aromatic L-amino acid decarboxylase (AADC), a vitamin B6-requiring enzyme that converts L-dopa to dopamine and 5-hydroxytryptophan to serotonin. Deficiency of this enzyme results in developmental delay, muscular hypotonia, dystonia, involuntary movements, autonomic dysfunction, and oculogyric crises...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Medknow Publications & Media Pvt Ltd
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4090859/ https://www.ncbi.nlm.nih.gov/pubmed/25024584 http://dx.doi.org/10.4103/0972-2327.132652 |
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author | Gücüyener, Kıvılcım Kasapkara, Çiğdem Seher Tümer, Leyla Verbeek, Marcel M. |
author_facet | Gücüyener, Kıvılcım Kasapkara, Çiğdem Seher Tümer, Leyla Verbeek, Marcel M. |
author_sort | Gücüyener, Kıvılcım |
collection | PubMed |
description | Aromatic L-amino acid decarboxylase (AADC), a vitamin B6-requiring enzyme that converts L-dopa to dopamine and 5-hydroxytryptophan to serotonin. Deficiency of this enzyme results in developmental delay, muscular hypotonia, dystonia, involuntary movements, autonomic dysfunction, and oculogyric crises. We now report a 2-year-old Turkish boy with AADC deficiency confirmed by greatly reduced AADC activity in the plasma and by genetic studies. Mutation analysis revealed a homozygous mutation c.208C > T (p. His70Tyr) in exon 3 of the AADC gene which has not been described to date. |
format | Online Article Text |
id | pubmed-4090859 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-40908592014-07-14 Aromatic L-Amino acid decarboxylase deficiency: A new case from Turkey with a novel mutation Gücüyener, Kıvılcım Kasapkara, Çiğdem Seher Tümer, Leyla Verbeek, Marcel M. Ann Indian Acad Neurol Case Report Aromatic L-amino acid decarboxylase (AADC), a vitamin B6-requiring enzyme that converts L-dopa to dopamine and 5-hydroxytryptophan to serotonin. Deficiency of this enzyme results in developmental delay, muscular hypotonia, dystonia, involuntary movements, autonomic dysfunction, and oculogyric crises. We now report a 2-year-old Turkish boy with AADC deficiency confirmed by greatly reduced AADC activity in the plasma and by genetic studies. Mutation analysis revealed a homozygous mutation c.208C > T (p. His70Tyr) in exon 3 of the AADC gene which has not been described to date. Medknow Publications & Media Pvt Ltd 2014 /pmc/articles/PMC4090859/ /pubmed/25024584 http://dx.doi.org/10.4103/0972-2327.132652 Text en Copyright: © Annals of Indian Academy of Neurology http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Report Gücüyener, Kıvılcım Kasapkara, Çiğdem Seher Tümer, Leyla Verbeek, Marcel M. Aromatic L-Amino acid decarboxylase deficiency: A new case from Turkey with a novel mutation |
title | Aromatic L-Amino acid decarboxylase deficiency: A new case from Turkey with a novel mutation |
title_full | Aromatic L-Amino acid decarboxylase deficiency: A new case from Turkey with a novel mutation |
title_fullStr | Aromatic L-Amino acid decarboxylase deficiency: A new case from Turkey with a novel mutation |
title_full_unstemmed | Aromatic L-Amino acid decarboxylase deficiency: A new case from Turkey with a novel mutation |
title_short | Aromatic L-Amino acid decarboxylase deficiency: A new case from Turkey with a novel mutation |
title_sort | aromatic l-amino acid decarboxylase deficiency: a new case from turkey with a novel mutation |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4090859/ https://www.ncbi.nlm.nih.gov/pubmed/25024584 http://dx.doi.org/10.4103/0972-2327.132652 |
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